病例报告：双子宫畸形合并肾缺如导致的单侧阴道积血。
Case report: unilateral haematocolpos in uterine duplication associated with renal agenesis.
作者信息
Berman L, Stringer D A, St Onge O, Daneman A, Smith C
机构信息
Department of Radiology, Hospital for Sick Children, Toronto, Ontario, Canada.
出版信息
Clin Radiol. 1987 Sep;38(5):545-7. doi: 10.1016/s0009-9260(87)80152-6.
PMID:3311566
Abstract
A case of unilateral haematocolpos correctly diagnosed by ultrasound is described in a 13 year old girl known to have a solitary kidney. The association of renal agenesis with Müllerian abnormalities is well recognised and in this case the ultrasound findings ensured that the correct surgical management was undertaken.
摘要
本文描述了一例13岁已知患有单肾的女孩，其单侧阴道积血通过超声得以正确诊断。肾发育不全与苗勒氏管异常的关联已得到充分认识，在该病例中，超声检查结果确保了采取正确的手术治疗措施。
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